The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
71661338 7166133 8 F 20120906 20121228 20091103 20121231 EXP PHHY2009CA46396 NOVARTIS 82.41 YR M Y 0.00000 20121231 OT CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
71661338 7166133 1 PS ZOMETA 1 INTRAVENOUS 3.5 MG, EVERY 12 WEEKS U 21223 3.5 MG Solution For Injection

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
71661338 7166133 1 Prostate cancer

Outcome of event

Event ID CASEID OUTC COD
71661338 7166133 DE
71661338 7166133 HO
71661338 7166133 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
71661338 7166133 Asthenia
71661338 7166133 Blood pressure diastolic decreased
71661338 7166133 Blood testosterone decreased
71661338 7166133 Death
71661338 7166133 Hypophagia
71661338 7166133 Malaise
71661338 7166133 Muscle atrophy
71661338 7166133 Nausea
71661338 7166133 Prostatic specific antigen increased
71661338 7166133 Terminal state
71661338 7166133 Vomiting
71661338 7166133 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
71661338 7166133 1 20070714 20120111 0